Full data view for gene USH2A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_206933.2 transcript reference sequence.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+/+ 16 c.3309C>A r.(?) p.(Tyr1103*) Fibronectin type-III 1 (1058-1143) Parent #1 - pathogenic g.216380622G>T g.216207280G>T - - USH2A_000908 Heterozygous PubMed: Dad 2015, PubMed: Dad 2016 - rs397518011 Germline - - - - - DNA MLPA, SEQ - - USH2 USH2-5 (D61);USH2-5 (D61) PubMed: Dad 2015, PubMed: Dad 2016 Proband F - - - - - - - 1 Shzeena Dad
+/+ 16 c.3309C>A r.(?) p.(Tyr1103*) Fibronectin type-III 1 (1058-1143) Parent #1 - pathogenic g.216380622G>T g.216207280G>T - - USH2A_000908 Heterozygous; mutation PubMed: Bonnet 2016 - rs397518011 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/. - c.3309C>A r.(?) p.(Tyr1103Ter) - Unknown - pathogenic g.216380622G>T g.216207280G>T - - USH2A_000908 - PubMed: Zhao 2015 - - Germline - - - - - DNA SEQ-NG - 86-gene panel retinal disease Rp311B PubMed: Zhao 2015 simplex case - - Northern Ireland - - - - - 1 LOVD
+/. - c.3309C>A r.(?) p.(Tyr1103*) - Parent #2 - pathogenic g.216380622G>T g.216207280G>T USH2A allele 1: Exon 10 deletion, g.216462804_ 216472385del, allele 2: p.Tyrll03X - USH2A_000908 - PubMed: Austin-Tse 2018 SCV000065521 - Germline yes - - - - DNA SEQ-NG-I, arrayCGH - sequenced by dideoxy sequencing or hearing loss gene panel by either microarray-based resequencing or oligonucleotide-based target capture followed by next generation sequencing using Illumina HiSeq2000 or MiSeq instrument USH R-2 PubMed: Austin-Tse 2018 Retrospective Cohort ? - United States - - - - - 1 LOVD
+/. 16 c.3309C>A r.(?) p.(Tyr1103*) - Parent #1 ACMG pathogenic g.216380622G>T g.216207280G>T USH2A c.C3309A, p.Y1103* - USH2A_000908 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF1120 PubMed: Zhu 2021 family 157, patient SRF1120 F - China - - - - - 1 LOVD
+/. 16 c.3309C>A r.(3309c>a) p.(Tyr1103Ter) - Parent #1 ACMG pathogenic g.216380622G>T g.216207280G>T - - USH2A_000908 no variant 2nd chromome PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP18 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+?/. - c.3309C>A r.(?) p.(Tyr1103Ter) - Unknown ACMG likely pathogenic g.216380622G>T g.216207280G>T - - USH2A_000908 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Dad, S. et al., 2015; PubMed: Bonnet, C. et al., 2016 - rs397518011 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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